Organelle degradation during the lens and erythroid differentiation is independent of autophagy

被引:94
作者
Matsui, M
Yamamoto, A
Kuma, A
Ohsumi, Y
Mizushima, N [1 ]
机构
[1] Tokyo Metropolitan Inst Med Sci, Dept Bioregulat & Metab, Tokyo 1138613, Japan
[2] Grad Inst Adv Studies, Sch Life Sci, Dept Basic Biol, Okazaki, Aichi 4448585, Japan
[3] Natl Inst Basic Biol, Dept Cell Biol, Okazaki, Aichi 4448585, Japan
[4] Nagahama Inst Biosci & Technol, Dept Biosci, Nagahama 5260829, Japan
[5] Japan Sci & Technol Agcy, PRESTO, Kawaguchi 3320012, Japan
关键词
autophagy; lens; erythroid cell; organelle degradation; lysosome;
D O I
10.1016/j.bbrc.2005.11.044
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Autophagy is a bulk degradation system within cells through which cytoplasmic components are degraded within lysosomes. Primary roles of autophagy are starvation adaptation and intracellular protein quality control. In contrast to the ubiquitin-proteasome system, autophagy can also degrade organelles. Here we examined a possible role of autophagy in organelle degradation during lens and erythroid differentiation. We observed that autophagy occurs in embryonic lens cells. However, organelle degradation in lens and erythroid cells occurred normally in autophagy-deficient Atg5(-/-) mice. Our data suggest that degradation system(s) other than autophagy play major roles in organelle degradation during these processes. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:485 / 489
页数:5
相关论文
共 34 条
[1]   Lens organelle degradation [J].
Bassnett, S .
EXPERIMENTAL EYE RESEARCH, 2002, 74 (01) :1-6
[2]   Autophagy: in sickness and in health [J].
Cuervo, AM .
TRENDS IN CELL BIOLOGY, 2004, 14 (02) :70-77
[3]  
David L L, 1989, Lens Eye Toxic Res, V6, P725
[4]   Subcellular redistribution of components of the ubiquitin-proteasome pathway during lens differentiation and maturation [J].
Girao, H ;
Pereira, P ;
Taylor, A ;
Shang, F .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2005, 46 (04) :1386-1392
[5]   Starvation triggers the delivery of the endoplasmic reticulum to the vacuole via autophagy in yeast [J].
Hamasaki, M ;
Noda, T ;
Baba, M ;
Ohsumi, Y .
TRAFFIC, 2005, 6 (01) :56-65
[6]   AUTOPHAGY OF MITOCHONDRIA IN RAT BONE-MARROW ERYTHROID-CELLS - RELATION TO NUCLEAR EXTRUSION [J].
HEYNEN, MJ ;
TRICOT, G ;
VERWILGHEN, RL .
CELL AND TISSUE RESEARCH, 1985, 239 (01) :235-239
[7]   BOVINE LENS EPITHELIAL-CELLS HAVE A UBIQUITIN-DEPENDENT PROTEOLYSIS SYSTEM [J].
HUANG, LL ;
JAHNGENHODGE, J ;
TAYLOR, A .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1175 (02) :181-187
[8]   A ubiquitin-like system mediates protein lipidation [J].
Ichimura, Y ;
Kirisako, T ;
Takao, T ;
Satomi, Y ;
Shimonishi, Y ;
Ishihara, N ;
Mizushima, N ;
Tanida, I ;
Kominami, E ;
Ohsumi, M ;
Noda, T ;
Ohsumi, Y .
NATURE, 2000, 408 (6811) :488-492
[9]   LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing [J].
Kabeya, Y ;
Mizushima, N ;
Uero, T ;
Yamamoto, A ;
Kirisako, T ;
Noda, T ;
Kominami, E ;
Ohsumi, Y ;
Yoshimori, T .
EMBO JOURNAL, 2000, 19 (21) :5720-5728
[10]  
KENT G, 1966, AM J PATHOL, V48, P831